Cas no 19451-11-7 (Iodocyclopropane)
Iodocyclopropane Chemical and Physical Properties
Names and Identifiers
-
- Cyclopropane, iodo-
- Cyclopropyl iodide
- Iodocyclopropane
- 1-Iodocyclopropane
- cyclopropyliodide
- VLODBNNWEWTQJX-UHFFFAOYSA-N
- InChI=1/C3H5I/c4-3-1-2-3/h3H,1-2H
- MFCD20621267
- AKOS024462864
- AC5127
- SY046875
- A936748
- BS-12655
- 1-Iodocyclopropane; Iodocyclopropane pound>>Cyclopropyliodide
- SCHEMBL1354775
- 19451-11-7
- BCP29363
- EN300-214303
-
- MDL: MFCD20621267
- Inchi: 1S/C3H5I/c4-3-1-2-3/h3H,1-2H2
- InChI Key: VLODBNNWEWTQJX-UHFFFAOYSA-N
- SMILES: IC1CC1
Computed Properties
- Exact Mass: 167.94315
- Monoisotopic Mass: 167.94360g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 4
- Rotatable Bond Count: 0
- Complexity: 22.5
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 0
- XLogP3: 2.1
Experimental Properties
- PSA: 0
Iodocyclopropane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM328355-25g |
iodocyclopropane |
19451-11-7 | 95%+ | 25g |
$9016 | 2022-09-01 | |
| abcr | AB521910-250 mg |
Iodocyclopropane; . |
19451-11-7 | 250MG |
€424.50 | 2023-04-17 | ||
| abcr | AB521910-1 g |
Iodocyclopropane; . |
19451-11-7 | 1g |
€997.40 | 2023-04-17 | ||
| TRC | I707015-10mg |
iodocyclopropane |
19451-11-7 | 10mg |
$ 50.00 | 2022-06-04 | ||
| TRC | I707015-50mg |
iodocyclopropane |
19451-11-7 | 50mg |
$ 210.00 | 2022-06-04 | ||
| TRC | I707015-100mg |
iodocyclopropane |
19451-11-7 | 100mg |
$ 295.00 | 2022-06-04 | ||
| Chemenu | CM328355-1g |
iodocyclopropane |
19451-11-7 | 95%+ | 1g |
$923 | 2023-02-17 | |
| Chemenu | CM328355-5g |
iodocyclopropane |
19451-11-7 | 95%+ | 5g |
$2769 | 2023-02-17 | |
| Enamine | EN300-214303-0.05g |
iodocyclopropane |
19451-11-7 | 95% | 0.05g |
$105.0 | 2023-09-16 | |
| Enamine | EN300-214303-0.1g |
iodocyclopropane |
19451-11-7 | 95% | 0.1g |
$156.0 | 2023-09-16 |
Iodocyclopropane Suppliers
Iodocyclopropane Related Literature
-
Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
-
Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
-
Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
Additional information on Iodocyclopropane
Iodocyclopropane (CAS No. 19451-11-7): An Overview of Its Properties, Applications, and Recent Research Advances
Iodocyclopropane (CAS No. 19451-11-7) is a cyclic organic compound characterized by its unique molecular structure, which consists of a three-membered ring with an iodine atom attached. This compound has garnered significant attention in the fields of organic chemistry, medicinal chemistry, and materials science due to its potential applications and intriguing chemical properties.
The molecular formula of iodocyclopropane is C3H5I, and its molecular weight is approximately 152.07 g/mol. The compound's high reactivity and unique electronic properties make it a valuable intermediate in various synthetic pathways. In recent years, researchers have explored the use of iodocyclopropane in the synthesis of complex organic molecules, particularly those with biological relevance.
Iodocyclopropane exhibits notable reactivity due to the strain inherent in the three-membered ring and the presence of the iodine atom. This strain can be harnessed to facilitate ring-opening reactions, which are crucial in the synthesis of a wide range of compounds. For instance, studies have shown that iodocyclopropane can undergo ring-opening reactions with nucleophiles such as amines and thiols, leading to the formation of substituted propargylamines and propargylthiols, respectively.
In the realm of medicinal chemistry, iodocyclopropane has been investigated for its potential as a building block in the development of novel drugs. The iodine atom can serve as a handle for further functionalization, allowing chemists to introduce various substituents that can modulate the biological activity of the final product. Recent research has focused on using iodocyclopropane-derived compounds in the design of inhibitors for specific enzymes and receptors, which could have therapeutic applications in diseases such as cancer and neurodegenerative disorders.
Beyond its use in medicinal chemistry, iodocyclopropane has also found applications in materials science. The compound's reactivity and ability to form stable derivatives make it an attractive candidate for the synthesis of functional materials with tailored properties. For example, researchers have explored the use of iodocyclopropane-based polymers in the development of advanced materials for electronic and optical devices.
The environmental impact of chemical compounds is an increasingly important consideration in their development and application. Studies on the environmental fate and toxicity of iodocyclopropane are limited but ongoing. Preliminary data suggest that while iodocyclopropane is not highly toxic at low concentrations, its reactivity may pose risks if not handled properly. Therefore, appropriate safety measures should be taken during its synthesis and use.
In conclusion, iodocyclopropane (CAS No. 19451-11-7) is a versatile compound with a wide range of applications in organic synthesis, medicinal chemistry, and materials science. Its unique chemical properties make it an important intermediate in various synthetic pathways, and ongoing research continues to uncover new possibilities for its use. As research progresses, it is likely that iodocyclopropane-based compounds will play an increasingly significant role in advancing scientific knowledge and developing innovative solutions to real-world problems.
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